NMT
- Product code
- NMT
- Device name
- Needle, Catheter, Reprocessed
- Device class
- Class 1
- 21 CFR
- 21 CFR 878.4200
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- Flag
- Third-party review eligible
FDA classification definition
Reprocessing validation data for this device type must be included in a 510(k) submission. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).
Official FDA classification page: NMT
Classification and pathway per current FDA publications. Data from openFDA (CC0).